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Conformis Hip System

FDA UDI

Class I (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
Conformis Hip System FDA UDI
Generic Name
Bone-resection orthopaedic reamer, single-use FDA UDI
Device Name
HIP-REAMER STAGE 1-44MM FDA UDI
Model / Reference
HAR000S14401 FDA UDI
Description
HIP-REAMER STAGE 1-44MM FDA UDI

Identifiers

Catalog Number
HAR000S144 FDA UDI
Primary DI / UDI-DI
M572HAR000S144011 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Bone-resection orthopaedic reamer, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 44 Millimeter FDA UDI

Category: Bone-resection orthopaedic reamer, single-use

Conformis Hip System by Conformis, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-resection orthopaedic reamer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI 01b3ff55-0482-4e2f-b2b7-c10e1e2c6cd1 35 fields · synced May 30, 2026